Table of Contents

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q

(Mark One)

x

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended September 30, 2017March 31, 2024

OR

¨

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ___​ ​ to ___​ ​

Commission file number 0-12957001-36435

Enzon Pharmaceuticals, Inc.

(Exact name of registrant as specified in its charter)

Delaware
22-2372868

Delaware

22-2372868

(State of incorporation)

(I.R.S. Employer Identification No.)

20 Commerce Drive (Suite 135), Cranford, New Jersey

07016

(Address of principal executive offices)

(Zip Code)

(732) (732) 980-4500

(Registrant’s telephone number, including area code)

Not Applicable

(Former name, former address and former fiscal year, if changed since last report)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading Symbol(s)

Name of each exchange on which registered

None

N/A

N/A

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports) and (2) has been subject to such filing requirements for the past 90 days. Yes x No ¨

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes x No ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer”filer,” “smaller reporting company,” and “smaller reporting“emerging growth company” in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filer ¨

Accelerated filer ¨

Non-accelerated filer ¨

Smaller reporting company x

Emerging growth company ¨

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.¨

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ¨ No x

Shares of Common Stock outstanding as of October 31, 2017: 44,214,603May 3, 2024: 74,214,603

Table of Contents

ENZON PHARMACEUTICALS, INC.

Table of Contents

Page

PART I - FINANCIAL INFORMATION

3

Item 1.

Financial Statements

3

Item 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

14

Item 3.

Quantitative and Qualitative Disclosures About Market Risk

18

Item 4.

Controls and Procedures

18

PART II – OTHER INFORMATION

19

Item 1.

Legal Proceedings

19

Item 1A.

Risk Factors

19

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

19

Item 3.

Defaults Upon Senior Securities

19

Item 4.

Mine Safety Disclosures

19

Item 5.

Other Information

19

Item 6.

Exhibits

19

Signatures

20

2

Table of Contents

PART I – FINANCIAL INFORMATION

Item 1. Financial Statements.

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED BALANCE SHEETS

(In thousands, except share and per share amounts)

  September 30,
2017
  December 31,
2016
 
  (Unaudited)    
ASSETS        
         
Current assets:        
Cash $4,320  $7,639 
Other receivable  3,500   - 
Other current assets  84   270 
Total current assets  7,904   7,909 
Deferred tax assets, net  1,149   3,362 
         
Total assets $9,053  $11,271 
         
LIABILITIES AND STOCKHOLDERS’ EQUITY        
         
Current liabilities:        
Accounts payable $213  $770 
Accrued expenses and other current liabilities  158   170 
         
Total current liabilities  371   940 
         
Commitments and contingencies        
         
Stockholders’ equity:        
Preferred stock - $0.01 par value, authorized 3,000,000 shares; no shares issued and outstanding at
   September 30, 2017 and December 31, 2016
  -   - 
Common stock - $0.01 par value, authorized 170,000,000 shares; issued and outstanding 44,214,603
   shares at September 30, 2017 and December 31, 2016
  441   441 
Additional paid-in capital  83,650   90,282 
Accumulated deficit  (75,409)  (80,392)
Total stockholders’ equity  8,682   10,331 
Total liabilities and stockholders’ equity $9,053  $11,271 

    

March 31, 

    

December 31, 

2024

2023

    

(Unaudited)

    

ASSETS

 

  

 

  

Current assets:

 

  

 

  

Cash and cash equivalents

$

45,988

$

47,012

Other current assets

 

481

 

331

Total current assets

46,469

47,343

Deferred tax asset

360

359

Total assets

$

46,829

$

47,702

LIABILITIES AND STOCKHOLDERS’ EQUITY

 

Current liabilities:

 

Accounts payable

$

331

$

331

Accrued expenses and other current liabilities

 

190

108

Dividends payable on Series C preferred stock

1,275

Total current liabilities

521

1,714

 

Commitments and contingencies

 

Mezzanine equity:

Series C preferred stock - $0.01 par value, 40,000 shares authorized, issued and outstanding (liquidation value $1,075 and $1,062 per share) at March 31, 2024 and December 31, 2023

43,014

42,483

Stockholders’ equity:

 

Preferred stock - $0.01 par value, authorized 2,960,000 shares; no shares issued and outstanding at March 31, 2024 and December 31, 2023

 

Common stock - $0.01 par value, authorized 170,000,000 shares; issued and outstanding 74,214,603 shares at March 31, 2024 and December 31, 2023

 

742

742

Additional paid-in capital

 

72,902

73,433

Accumulated deficit

 

(70,350)

(70,670)

Total stockholders’ equity

 

3,294

3,505

Total liabilities, mezzanine equity and stockholders’ equity

$

46,829

$

47,702

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 2

3

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(In thousands, except per share amounts)

(Unaudited)

  Three months ended  Nine months ended 
  September 30,  September 30, 
  2017  2016  2017  2016 
Revenues:                
Royalties $151  $1,965  $8,366  $7,461 
Miscellaneous income  -   21   -   63 
Total revenues  151   1,986   8,366   7,524 
                 
Operating expenses:                
General and administrative  335   376   1,021   1,533 
Total operating expenses  335   376   1,021   1,533 
                 
Operating (loss) income and (loss) income before income tax (benefit) expense  (184)  1,610   7,345   5,991 
                 
Income tax (benefit) expense  (337)  674   2,362   2,503 
Net income $153 $936  $4,983  $3,488 
                 
Earnings per common share                
Basic $0.00  $0.02  $0.11  $0.08 
Diluted $0.00  $0.02  $0.11  $0.08 
                 
Weighted-average shares – basic  44,215   44,214   44,215   44,214 
Weighted-average shares – diluted  44,215   44,214   44,215   44,214 

Three months ended

March 31, 

    

2024

    

2023

Revenues:

Royalties and milestones, net

$

$

Total revenues

 

Operating expenses:

 

General and administrative

 

326

285

Total operating expenses

 

326

285

Operating loss

 

(326)

(285)

Interest and dividend income

647

447

Income before income tax benefit

321

162

Income tax (expense) benefit

 

(1)

35

Net income

320

197

Dividends on Series C preferred stock

(531)

(531)

Net loss available to common shareholders

$

(211)

$

(334)

Loss per common share

Basic and diluted

$

(0.00)

$

(0.00)

Weighted average number of common shares

Basic and diluted

 

74,215

74,215

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 3

4

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWSMEZZANINE EQUITY AND STOCKHOLDERS’ EQUITY

(In thousands)

(Unaudited)

  Nine months ended
September 30,
 
  2017  2016 
       
Cash flows from operating activities:        
Net income $4,983  $3,488 
Adjustments to reconcile net income to net cash provided by operating activities:        
Deferred tax provision  2,213   2,501 
Changes in operating assets and liabilities  (3,883)  (4,765)
Net cash provided by operating activities  3,313   1,224 
         
Cash flows from financing activities:        
Common stock dividend  (6,632)  - 
Net cash used in financing activities  (6,632)  - 
         
Net (decrease) increase in cash  (3,319)  1,224 
         
Cash at beginning of period  7,639   11,672 
         
Cash at end of period $4,320  $12,896 

Mezzanine Equity – Series C

Preferred Stock

Common Stock

Additional

Total

Number of

Par

Number of

Par

Paid-in

Accumulated

Stockholders’

    

Shares

    

Value

  

  

Shares

    

Value

    

Capital

    

Deficit

    

Equity

Balance, December 31, 2022

40

42,483

74,215

$

742

$

74,708

$

(72,043)

$

3,407

Net income

197

197

Preferred stock dividend accumulation

 

531

(531)

(531)

Balance, March 31, 2023

40

$

43,014

74,215

$

742

$

74,177

$

(71,846)

$

3,073

Mezzanine Equity – Series C

Preferred Stock

Common Stock

Additional

Total

Number of

Par

Number of

Par

Paid-in

Accumulated

Stockholders’

    

Shares

    

Value

  

  

Shares

    

Value

    

Capital

    

Deficit

    

Equity

Balance, December 31, 2023

40

42,483

74,215

$

742

$

73,433

$

(70,670)

$

3,505

Net income

320

320

Preferred stock dividend accumulation

531

(531)

(531)

Balance, March 31, 2024

 

40

$

43,014

74,215

$

742

$

72,902

$

(70,350)

$

3,294

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 4

5

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands)

(Unaudited)

Three months ended

March 31, 

    

2024

    

2023

Cash flows from operating activities:

Net income

$

320

$

197

Adjustments to reconcile net income to net cash provided by operating activities:

 

Deferred income taxes

 

(1)

(36)

Changes in operating assets and liabilities

(68)

9

Net cash provided by operating activities

 

251

170

Cash flows from financing activities:

 

Preferred stock dividend payments

(1,275)

(1,275)

Net cash used in financing activities

 

(1,275)

(1,275)

Net decrease in cash and cash equivalents

 

(1,024)

(1,105)

Cash and cash equivalents, beginning of period

 

47,012

46,982

Cash and cash equivalents, end of period

$

45,988

$

45,877

Non-cash financing activities:

Accretion of dividend for Series C Preferred Stock

$

531

$

531

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

6

Table of Contents

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(1)Description of Business

Enzon Pharmaceuticals, Inc. (together with its subsidiaries, “Enzon”the “Company,” “Enzon,” “we” or “us”) is positioned as a public company acquisition vehicle, where it can become an acquisition platform and potentially utilize its net operating loss carryforwards (“NOLs”) in an effort to enhance stockholder value.

In September 2020, the “Company”Company initiated a rights offering for its common and preferred stock (see below and Note 12 to our Condensed Consolidated Financial Statements), which closed in October 2020, and it realized $43.6 million in gross proceeds. This has enabled the Company to embark on its plan to potentially realize the value of its more than $100 million NOLs by acquiring businesses or assets. To protect the NOLs, in August 2020, the Company’s Board of Directors (the “Board”) receivesadopted a Section 382 rights plan (see Note 11 to our Condensed Consolidated Financial Statements).

Historically, the Company had received royalty revenues from existing licensing arrangements with other companies primarily related to sales of four marketedcertain drug products namely, PegIntron®, Sylatron®, Macugen® and CIMZIA®. The primary source ofthat utilized Enzon’s proprietary technology. In recent years, the Company’s royalty revenues in 2017 is the entrance into a Second Amendment (“Nektar Second Amendment”) to the Company’s Cross-License and Option Agreement (the “Nektar License Agreement”) withNektar Therapeutics, Inc. (“Nektar”), which generated non-recurring royalty revenues of $7 million in the nine months ended September30, 2017 (see below).

Previously, the primary source of the Company’s royalty revenues was sales of PegIntron, which is marketed by Merck & Co., Inc. (“Merck”). The Company currently has had no clinical operations and limited corporate operations. Enzon has a marketing agreement in the drug Vicineum, which, if approved, would, potentially, generate milestone and royalty payments to it in the future. Enzon cannot assure you that it will earn material future royalties or milestones.

The Company has no intention of resuming any clinical development activities or acquiring new sources of royalty revenues. Royalty revenues from sales of PegIntron accounted for approximately 100%Board and 61% of the Company’s total royalty revenues for the three months ended September 30, 2017management are actively involved in pursuing, sourcing, reviewing and 2016, respectively,evaluating various potential acquisition transactions consistent with its strategy. The Company’s management and approximately 13%Board have made a number of contacts and 70%engaged in discussions with principals of the Company’s total royalty revenueindividual companies and financial advisors on behalf of various individual companies, while continuing to evaluate potential transactions. To date, no acquisition candidates have been identified that are in the nine-month periods ended September 30, 2017 and 2016, respectively, before adjustment for Merck’s recoupment of previously overpaid royalties. The effects of such recoupments were recorded as decreases of royalty revenues aggregating $0 and $564,000 for the three and nine-month periods ending September 30, 2017, respectively, as discussed in Note 11.

an actionable state.

The Company was previously dedicated to the research and development of innovative therapeutics for patientshas a marketing agreement with high unmet medical needs. Beginning in December 2012, the Company’s Board of Directors (the “Board”), with outside consultants, began a review of the possible sale or disposition of one or more corporate assets or a sale of the Company. At that time, the Company suspended substantially all clinical development activities with a goal of conserving capital and maximizing value returned to the Company’s stockholders.   By April 2013, the review did not result in a definitive offer to acquire the Company or all or substantially all of the Company’s assets.  At the same time, the Company announced that its Board intended to distribute excess cash, expected to arise from ongoing royalty revenues, in the form of periodic dividends to stockholders.  On February 4, 2016, the Company’s Board adopted a Plan of Liquidation and Dissolution, the implementation of which has been postponed. (See Note 10.)

Under the Company’s existing agreements with certain third party licensees, the Company may be entitled to (i) potential future milestone payments contingent upon the achievement of certain milestones with respect to several other drug products in various stages of clinical and preclinical development and (ii) potential future royalty payments related to any future sales of these drug products.  Due to the challenges associated with developing and obtaining approval for drug products, there is substantial uncertainty whether any of these milestones will be achieved.  The Company also has no control over the time, resources and effort that these third party licensees may devote to their programs and limited access to information regarding or resulting from such programs.   Accordingly, there can be no assurance that the Company will receive any of the milestone or royalty payments under these agreements. 

AsMicromet AG, now part of the Company’s sale of its former specialty pharmaceutical business that was completed in January 2010, the CompanyAmgen, Inc. (the “Micromet Agreement”), pursuant to which it may be entitled to certain potential future milestone and royalty payments contingent uponif Vicineum, a drug that was being developed by Sesen, Inc., (Sesen”) is approved for the achievementtreatment of certain regulatory approval-related milestonesnon-muscle invasive bladder cancer. Sesen announced that it had completed a merger with Carisma Therapeutics Inc. (“Carisma”) and that the combined company will focus on the advancement of Carisma’s proprietary cell therapy for the treatment of cancer and other disorders and that it intends to seek a partner for the further development of Vicineum.

In the past, through 2022, the Company received an annual license maintenance fee of approximately $26,000 from Amgen, Inc. in payment of a worldwide, royalty-free non-exclusive right to license Vicineum. The fee represents half of the amount paid by Viventia Biotech (Barbados) Inc. (“Viventia”), part of Sesen, on an annual basis for the continued right to license Vicineum. The Company did not receive any license maintenance fees in 2023 or through the first quarter of 2024.

In August 2020, the Board adopted a Section 382 rights plan and declared a dividend distribution of one right for each outstanding share of the Company’s common stock to stockholders of record at the close of business on August 24, 2020. (See Note 11 to the Consolidated Financial Statements.)

In September 2020, the Board approved a Rights Offering (the “Rights Offering”), by which the Company distributed, at no charge to all holders of its common stock on September 23, 2020 (the “Record Date”), transferable subscription rights to purchase units (“Units”) at a subscription price per Unit of $1,090. In the Rights Offering, each stockholder on the Record Date received one subscription right for every share of common stock owned on the Record Date. For every 1,105 subscription rights held, a stockholder was entitled to purchase one Unit at the subscription price. Each Unit consisted of one share of newly designated Series C Preferred Stock, par value $0.01 per share, and 750 shares of the Company’s common stock. The subscription period for the Rights Offering ended on October 9, 2020.

As a result of the sale of all 40,000 Units available for purchase in the Rights Offering, the Company received approximately $43.6 million of gross proceeds and had 40,000 shares of Series C Preferred Stock outstanding and an aggregate of 74,214,603 shares of common stock outstanding following the Rights Offering. (See Note 12 to the Consolidated Financial Statements.)

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Table of Contents

ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(1)Description of Business (continued)

On an annual basis, the Board may, at its sole discretion, cause a dividend with respect to Oncaspar from Shire plc (“Shire”), which assumed the milestone payment obligations when it acquiredSeries C Preferred Stock to be paid in cash to the Oncaspar product portfolio from Sigma-Tau Finanziaria S.p.A.holders in July 2015. Based on Shire’s May 2, 2017 investor presentation, the Company believed that Shire anticipated filing a Biologics License Application (“BLA”) for SC Oncaspar with the FDA in the third quarter of 2017. As of September 30, 2017, there has been no public announcement by Shire of any such filing. If filed and FDA approval is obtained for SC Oncaspar, under its agreement, the Company would be entitledan amount equal to a milestone payment of $7.0 million. There can be no assurance that Shire will file a BLA for SC Oncaspar with the FDA or that the FDA will approve the BLA, if filed.  Accordingly, there can be no assurance that the Company will receive any3% of the milestone payments relatedliquidation preference as in effect at such time (initially $1,000 per share). If the dividend is not so paid in cash, the liquidation preference is adjusted and increased annually by an amount equal to SC Oncaspar5% of the liquidation preference per share as in effect at such time, that is not paid in cash to the holders on such date. The Board did not declare a dividend as of December 31, 2021 and, at December 31, 2021 the liquidation value of the Series C Preferred Stock was $1,062 per share. On December 29, 2022, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating $1,275,000 or any other such milestone payments resulting from its agreements with any$31.86 per share. Accordingly, the cumulative liquidation value of the Series C Preferred Stock remained at approximately $42,483,000 ($1,062 per share) on December 31, 2022. On December 28, 2023, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating approximately $1,275,000 or $31.86 per share. Accordingly, the cumulative liquidation value of the Series C Preferred Stock remained at approximately $42,483,000 ($1,062 per share) on December 31, 2023. The dividend was paid on January 17, 2024 to the holders of record of the Company’s other third party licensees. The Company will not recognize revenue until notification from Shire oranySeries C Preferred Stock as of the Company’s other third party licensees that the conditions necessitating payment of the milestone were satisfied and collection of the milestone payment is reasonably assured.

On June 26, 2017, the Company entered into the Nektar Second Amendment, wherein Nektar agreed to buy-out all remaining payment obligationsJanuary 10, 2024. (See Note 13 to the Company underConsolidated Financial Statements.)

As of March 31, 2024, the Nektar License Agreement. In consideration for fully paid-up licenses underBoard had not yet determined whether to declare a cash dividend at the Nektar License Agreement and for the dismissal with prejudiceend of all claims and counterclaims asserted in the litigation with Nektar, Nektar agreed to pay the Company the sum of $7.0 million, which satisfies all future obligations of royalty payments pursuant to the Nektar License Agreement, the first $3.5 million of which was paid within one business day of the effective date of the Nektar Second Amendment and the remaining $3.5 million will be paid within one business day of January 5, 2018.2024. Accordingly, the Company recorded revenueaccrued an accretion at 5% for the quarter on a pro rata basis (approximately $531,000 or $13 per share) and, as a result, the liquidation value of $7.0 million andthe Series C Preferred Stock was approximately $43,014,000 ($1,075 per share) at March 31, 2024. (See Note 13 to the Condensed Consolidated Financial Statements.)

The Company maintains its principal executive offices at 20 Commerce Drive, Suite 135, Cranford, New Jersey 07016 through a receivable of $3.5 million in the second quarter of 2017.service agreement with Regus Management Group, LLC.

 5

(2)Basis of Presentation

Interim Financial Statements

The accompanying unaudited condensed consolidated financial statements have been prepared from the books and records of the Company in accordance with United States accounting principles generally accepted accounting principles (U.S. GAAP)in the United States of America (“U.S. GAAP”) for interim financial information and Rule 10-01 of Regulation S-X promulgated by the U.S. Securities and Exchange Commission.Commission (“SEC”). Accordingly, these financial statements do not include all of the information and footnotes required for complete annual financial statements. Interim results are not necessarily indicative of the results that may be expected for the full year. Interim condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and the notes thereto included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2016.2023.

Principles of Consolidation

The condensed consolidated financial statements include the accounts of the Company and its wholly owned subsidiaries. All intercompany balances and transactions have been eliminated as part of the consolidation.

Use of Estimates

The preparation of consolidated financial statements in conformity with U.S. GAAPaccounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect reported amounts of assets and liabilities, disclosures of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenues and expenses during the reporting period. These estimates include legal and contractual contingencies and income taxes. Although management bases its estimates on historical experience, relevant current information and various other assumptions that are believed to be reasonable under the circumstances, actual results could differ from these estimates.

8

Table of Contents

RevenuesENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(2)Basis of Presentation (continued)

Royalties underRevenue Recognition

Royalty revenues from the Company’s license agreements with third-partiesthird parties and pursuant to the sale of itsthe Company’s former specialty pharmaceutical business are recognized when the Company can reasonably determinabledetermine the amounts earned. In most cases, this will be upon notification from the third-party licensee, which is typically during the quarter following the quarter in which the sales occurred. The Company does not participate in the selling or marketing of products for which it receives royalties. Because the Company records revenue only when collection is assured, no provision for uncollectible accounts is established upon recognition of revenues.

Contingent payments with third parties and earned throughpursuant to the sale of the product byCompany’s former specialty pharmaceutical business are recognized as income when the third-partymilestone has been achieved and collection is reasonably assured. Notification fromassured, such payments are non-refundable and no further effort is required on the third-party licenseepart of the royalties earnedCompany or the other party to complete the earning process.

Income Taxes

Income taxes are accounted for under the license agreement isasset and liability method. Deferred tax assets and liabilities are recognized for the basis for royalty revenue recognition. This information generally is received fromestimated future tax consequences attributable to differences between the licenseesfinancial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the quarter subsequentyears in which those temporary differences are expected to be realized. The effect of a change in tax rates or laws on deferred tax assets and liabilities is recognized in operations in the period in whichthat includes the sales occur.

(3)    New Accounting Pronouncements

In May 2014, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2014-09, “Revenue from Contracts with Customers,” relating to revenue recognition.  This new standard provides for a single five-step model to be applied to all revenue contracts with customers as well as requires additional financial statement disclosures that will enable users to understand the nature, amount, timing and uncertainty of revenue and cash flows relating to customer contracts.  Companies have an option to use either a retrospective approach or cumulative effect adjustment approach to implement the standard.  This ASU, as amended, is effective for fiscal years and interim periods within those years beginning after December 15, 2017.  The Company is currently assessing the impact of this update, but preliminarily believes that its adoption will not have a material impact on the Company’s consolidated financial statements.

The Company does not expect the adoption of other recently issued accounting pronouncements to have a significant impact on the Company’s results of operations, financial position or cash flow.

(4)    Financial Instruments and Fair Value

The carrying values of cash, other receivables, other current assets, accounts payable, accrued expenses and other current liabilities in the Company’s condensed consolidated balance sheets approximated their fair values at September 30, 2017 and December 31, 2016 due to their short-term nature.

(5)    Supplemental Cash Flow Information

There were no income tax or interest payments made during the nine months ended September 30, 2017.

There were estimated federal income tax payments of $135,000 and estimated New Jersey income tax payments of $1,500 made during the nine months ended September 30, 2016. The $135,000 represented an over estimate of taxes due in the third quarter of 2016, such amount was recorded as a receivable, included in other current assets, and subsequently collected.

On August 10, 2017, the Company’s Board of Directors declared a special cash dividend of $0.15 per shareenactment date of the Company’s common stock.This dividend, aggregating approximately $6.6 million, was paid on September 26, 2017.

 6

(6)    Income Per Common Share

 Basic earnings per common sharerate change. A valuation allowance is computed by dividing the income availableestablished to common stockholders by the weighted-average number of shares of common stock outstanding during the period. Restricted stock units (nonvested shares) are not considered to be outstanding shares until the vesting criteria (service and/or performance) have been satisfied.

For purposes of calculating diluted earnings per common share, the denominator includes both the weighted-average number of shares of common stock outstanding and the number of common stock equivalents if the inclusion of such common stock equivalents is dilutive. Dilutive common stock equivalents potentially include stock options and nonvested shares using the treasury stock method and shares issuable under the employee stock purchase plan (ESPP). There were no common stock equivalents during any of the periods presented. Income per common share information is as follows (in thousands, except per share amounts):

  Three months ended
September 30,
  Nine months ended 
September 30,
 
  2017  2016  2017  2016 
Income Per Common Share – Basic and Diluted:                
Net income $ 153  $936  $4,983  $3,488 
                 
Weighted-average common shares outstanding  44,215   44,214   44,215   44,214 
                 
Basic and diluted income per share $ 0.00  $0.02  $0.11  $0.08 

As of September 30, 2017 and 2016, options for 41,787 and 218,719 shares, respectively, were outstanding that have been excluded from the calculation of diluted weighted average shares outstanding, as they would be anti-dilutive since the respective options’ strike price was greater than the current market price of the shares and/or there was a net loss for the three-month period ended September 30, 2017.

 7

(7)    Stock-Based Compensation

Stock Options and Restricted Stock Units (RSUs or Nonvested Shares)

During the nine months ended September 30, 2017 and 2016, no options were granted and the Company incurred no stock-based compensation expense. No RSUs were outstanding as of September 30, 2017.

Activity related to stock options and nonvested shares during the nine months ended September 30, 2017 and related balances outstanding as of that date are reflected below (in thousands):

Stock
Options
Outstanding at January 1, 2017219
Granted-
Exercised and vested-
Expired and forfeited177
Outstanding at September 30, 201742
Options vested and expected to vest at September 30, 201742
Options exercisable at September 30, 201742

 8

(8)    Income Taxes

The Company incurred tax expense of approximately $2.4 million for the nine months ended September 30, 2017 of which approximately $0.3 million in income tax benefit was incurred during the third quarter of 2017. The effective tax rate for the three-month period ended September 30, 2017 was 183% compared to 41.7% for the corresponding period in the prior year. The change in the rate is attributable to a pre-tax book loss for the quarter as well as changes in projected income for the year. The Company expects to continue to utilizereduce the deferred tax asset throughassets to the remainder of 2017, resulting in an expected effective tax rate of approximately 39.1% for the year.

 After reducing its deferred tax assets by approximately $2.2 million during nine months ended September 30, 2017, the Company continues to provide a valuation allowance against all of its deferred tax assets except for NOLs expected to be utilized in the 2018 and 2019 tax years as the Company believes it isamounts that are more likely than not that these remaining deferred tax assets will notto be realized. Management of the Company will continue to assess the need for this valuation allowance and will make adjustments to it when appropriate.realized from operations.

During the nine months ended September 30, 2016, the Company recorded $2.5 million of income tax expense for U.S. federal income tax, substantially all of which related to a reduction of the Company’s net deferred tax assets. Of this amount, approximately, $674,000 was recorded in the third quarter of 2016.

Tax benefits of uncertain tax positions are recognized only if it is more likely than not that the Company will be able to sustain a position taken on an income tax return. The Company has no liability for uncertain tax positions. Interest and penalties, if any, related to unrecognized tax benefits, would be recognized as income tax expense.

(3)Recent Accounting Pronouncements

Recent Accounting Standards Updates issued by the Financial Accounting Standards Board (the “FASB”) and guidance issued by the SEC did not, or are not believed by management to, have a material effect on the Company’s present or future consolidated financial statements.

(4)Financial Instruments and Fair Value

The carrying values of cash and cash equivalents, other current assets, accounts payable, accrued expenses and other current liabilities in the Company’s consolidated balance sheets approximated their fair values at March 31, 2024 and December 31, 2023 due to their short-term nature. As of each of March 31, 2024 and December 31, 2023, the Company held cash equivalents aggregating approximately $45.9 million and $47.0 million, respectively.

(5)Supplemental Cash Flow Information

The Company made no income tax payments during each of the three-month periods ended March 31, 2024 and 2023. There were no interest payments made during either of the three-month periods ended March 31, 2024 or 2023.

(6)Cash Dividend

On December 28, 2023, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating approximately $1,275,000 or $31.86 per share. Accordingly, the cumulative liquidation value of the Series C Preferred Stock was approximately $42,483,000 ($1,062 per share) on December 31, 2023. The dividend was paid on January 17, 2024 to the holders of record of the Company’s Series C Preferred Stock as of January 10, 2024 (See Note 13 to the Consolidated Financial Statements).

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ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(6)Cash Dividend (continued)

On December 29, 2022, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating approximately $1,275,000 or $31.86 per share. Accordingly, the cumulative liquidation value of the Series C Preferred Stock was approximately $42,483,000 ($1,062 per share) on December 31, 2022. The dividend was paid on January 17, 2023 to the holders of record of the Company’s Series C Preferred Stock as of January 10, 2023 (See Note 13 to the Condensed Consolidated Financial Statements).

(7)Loss Per Common Share

Basic earnings (loss) per common share (EPS) is calculated by dividing net income (loss), less any dividends, accretion or reduction or redemption on the Company’s Series C Preferred Stock, by the weighted average number of common shares outstanding during the reported period. Restricted stock awards and restricted stock units (collectively, “nonvested shares”) are not considered to be outstanding shares until the service or performance vesting period has been completed.

The diluted earnings per common share calculation would normally involve adjusting both the denominator and numerator as described here if the effect is dilutive.

For purposes of calculating diluted earnings per common share, the denominator normally includes both the weighted-average number of shares of common stock outstanding and the number of common stock equivalents if the inclusion of such common stock equivalents is dilutive. Dilutive common stock equivalents potentially include stock options and nonvested shares using the treasury stock method and shares issuable under the employee stock purchase plan. During each of the quarters ended March 31, 2024 and 2023, there were no common stock equivalents. There were no stock options or other equity-based incentives outstanding in either such period. Loss per common share information is as follows (in thousands, except per share amounts) for the three months ended March 31, 2024 and 2023:

Three months ended

March 31, 

    

2024

    

2023

Loss Per Common Share – Basic and Diluted:

Net income

$

320

$

197

Dividends on Series C preferred stock

(531)

(531)

Net loss available to common shareholders

$

(211)

$

(334)

Weighted-average common shares outstanding

 

74,215

74,215

Basic and diluted loss per share

$

(0.00)

$

(0.00)

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ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(8)Income Taxes

During the three-month period ended March 31, 2024 the Company recorded approximately $500 of income tax expense. During the comparable period in 2023, the Company recorded $34,500 of income tax benefit. The income tax benefit in the 2023 period was mainly related to a partial reversal of the valuation allowance on its deferred tax assets.

ASC 740 requires the reduction of deferred tax assets by a valuation allowance if, based on the weight of available evidence, it is more likely than not that some or all of the deferred tax assets will not be realized. Because of the inherent uncertainties, including future interest rates, whether or when an acquisition of a profitable entity will come to fruition and other factors, projecting long-term future performance of the Company is problematical. Accordingly, the Company is only projecting pre-tax book income through March 31, 2025 due to interest rates on its short-term cash investments and the absence of any potentially actionable acquisitions at this time. Upon review of positive and negative evidence in determining a partial reversal of the valuation allowance, the Company has concluded that a partial reversal of the valuation allowance is necessary. Interest rates may fluctuate throughout the period through March 31, 2025. However, the Company does not expect them to return to low rates of the past creating a projected taxable income position. Accordingly, a deferred tax benefit of $1,000 and $36,000 was recorded during the quarters ended March 31, 2024 and 2023, respectively. The Company may acquire businesses, entities or revenue streams that could generate sufficient income so that it can utilize its approximately $102.2 million NOL. To date, no acquisition candidates have been identified that are in an actionable state and, while the Company may ultimately be successful in realizing some or all of the value of its NOLs, the Company cannot provide assurance that it will be able to realize any value of its NOLs.

Management of the Company will continue to assess the need for this valuation allowance and will make adjustments when or if appropriate.

At March 31, 2024, the Company had federal NOLs of approximately $102.2 million, of which approximately $99.1 million will expire in the years 2025 through 2036, and New Jersey state NOLs of approximately $24.5 million that expire in the years 2031 through 2042. Under the Tax Cuts and Jobs Act, net operating losses generated in tax years beginning after December 31, 2017 have an unlimited carryforward period, and the amount of net operating loss allowed to be utilized each year is limited to 80% of taxable income.

At March 31, 2024, the Company has federal research and development (“R&D”) credit carryforwards of approximately $9.4 million that expire in the years 2024 through 2029. These deferred tax assets were subject to a valuation allowance such that the deferred tax expense incurred as a result of the expiration of the R&D credit carryforwards was offset by a corresponding deferred tax benefit for the related reduction in valuation allowance.

The Company's ability to use the NOLs and R&D tax credit carryforwards may be limited, as they are subject to certain limitations due to ownership changes as defined by rules pursuant to Section 382 of the Internal Revenue Code of 1986, as amended. However, management of the Company believes that the Company's NOLs will not be limited by any changes in the Company's ownership as a result of the successful completion of the Rights Offering. (See Note 12 to the Consolidated Financial Statements.) Additionally, in an effort to protect stockholder value by attempting to protect against a possible limitation on the Company's ability to use its NOLs, the Board adopted a Section 382 rights plan. (See Note 11 to the Consolidated Financial Statements.)

The Company has not recorded a liability for unrecognized income tax benefits.

(9)Commitments and Contingent Liabilities

Commencing on March 1, 2016, the Company changed the location of its principal executive offices to 20 Commerce Drive, Suite 135, Cranford, New Jersey, 07016. The Company entered into an office service agreement with Regus Management Group, LLC (“Regus”) for use of office space at this location effective March 1, 2016. Under the agreement, in exchange for the Company’s right to use the office space at this location,On January 17, 2024, the Company was required to pay Regus an initial service retainernotified by the OTCQX Markets Group (the “OTCQX”), the marketplace for the over-the-counter trading of $2,418 and thereafter pay Regusits stock, that it no longer met the standards for continued qualification for the OTCQX, in that its stock bid price had fallen below $0.10 per share for 30 consecutive calendar days. To regain compliance, the Company must maintain a monthly feeclosing bid price of $1,209 until February 28, 2017. This agreement was renewedat least $0.10 for another year, until February 28, 2018, for a monthly fee of $1,229.

10 consecutive trading days before July 15, 2024.

The Company has been involved in various claims and legal actions arising in the ordinary course of business. In the opinion of management, the ultimate disposition of these matters will not have a material effect on the Company’s consolidated financial position, results of operations, or liquidity.

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(10)    PlanAccounts Payable and Accrued Expenses

Prior to 2017, the Company’s primary source of Liquidationroyalty revenues was derived from sales of PegIntron, which is marketed by Merck & Co., Inc. (“Merck”). At December 31, 2023, we recorded a liability to Merck of approximately $331,000, based primarily on Merck’s assertions regarding recoupments related to prior returns and Dissolutionrebates. Merck has not yet reported royalty revenues earned by us for product sales and/or recoupments for returns and rebates for the quarter ended March 31, 2024. Accordingly, at March 31, 2024, the Company recorded a net payable to Merck of approximately $331,000 due to such royalty overpayment claims by Merck. The Company believes that it will receive no additional royalties from Merck.

Accrued expenses and other current liabilities consisted of the following as of March 31, 2024 and 2023 (in thousands):

    

March 31,

    

December 31,

    

2024

    

2023

Professional and consulting fees

$

184

$

92

Other

6

16

$

190

$

108

(11)Section 382 Rights Plan

On February 4, 2016,August 14, 2020, in an effort to protect stockholder value by attempting to protect against a possible limitation on the Company’s ability to use its NOLs, the Board adopted a PlanSection 382 rights plan and declared a dividend distribution of Liquidationone right for each outstanding share of the Company’s common stock to stockholders of record at the close of business on August 24, 2020. Accordingly, holders of the Company’s common stock own one preferred stock purchase right for each share of common stock owned by such holder. The rights are not immediately exercisable and Dissolution (the “Planwill become exercisable only upon the occurrence of Liquidationcertain events as set forth in the Section 382 rights plan. If the rights become exercisable, each right would initially represent the right to purchase from the Company one one-thousandth of a share of the Company’s Series A-1 Junior Participating Preferred Stock, par value $0.01 per share, for a purchase price of $1.20 per right. If issued, each fractional share of Series A-1 Junior Participating Preferred Stock would give the stockholder approximately the same dividend, voting and Dissolution”)liquidation rights as does one share of the Company’s common stock. However, prior to exercise, a right does not give its holder any rights as a stockholder of the Company, including any dividend, voting or liquidation rights. The rights will expire on the earliest of (i) the close of business on June 2, 2024 (unless that date is advanced or extended by the Board), pursuant to(ii) the time at which the Company would, subject to obtaining requisite stockholder approval, be liquidated and dissolved in accordance with Sections 280 and 281 (a)rights are redeemed or exchanged under the Section 382 rights plan, (iii) the close of business on the day of repeal of Section 382 of the General Corporation LawInternal Revenue Code or any successor statute or (iv) the close of business on the Statefirst day of Delaware. In approving the Plan of Liquidation and Dissolution, the Company’s Board had considered, among other factors, the abilitya taxable year of the Company to obtain no-action relief fromwhich the SECCompany’s Board of Directors determines that no NOLs may be carried forward.

(12)Rights Offering

On September 1, 2020, the Board approved a Rights Offering. For every 1,105 subscription rights held, a stockholder was entitled to suspend certainpurchase one Unit at the subscription price of $1,090. Each Unit consisted of one share of newly designated Series C Preferred Stock, par value $0.01 per share, and 750 shares of the Company’s reporting obligations undercommon stock. On October 9, 2020, the Securities Exchange ActRights Offering expired and, as a result of 1934,the sale of all 40,000 Units, the Company received approximately $43.6 million in gross proceeds and issued shares of Series C Preferred Stock and shares of common stock such that, following the closing of the Rights Offering, there was an aggregate of 40,000 shares of Series C Preferred Stock outstanding and 74,214,603 shares of common stock outstanding.

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ENZON PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(12)Rights Offering (continued)

On an annual basis, the Board may, at its sole discretion, cause a dividend with respect to the Series C Preferred Stock to be paid in cash to the holders in an amount equal to 3% of the liquidation preference as amended,in effect at such time (initially $1,000 per share). If the dividend is not so paid in cash, the liquidation preference is adjusted and increased annually by an amount equal to 5% of the liquidation preference per share as in effect at such time, that is not paid in cash to the holders on such date. Holders of Series C Preferred Stock do not have any voting rights and the anticipated cost savings ifSeries C Preferred Stock is not convertible into shares of the Company’s common stock. The initial liquidation value of the Series C Preferred Stock was $1,000 per share. At December 31, 2021 the liquidation value of the Series C Preferred Stock was $1,062 per share, inasmuch as no dividend was declared or paid in cash. On December 29, 2022, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating approximately $1,275,000 or $31.86 per share. Accordingly, the liquidation value of the Series C Preferred Stock was $1,062 per share on December 31, 2022. The dividend was paid on January 17, 2023 to the holders of record of the Company’s Series C Preferred Stock as of January 10, 2023. On December 28, 2023, the Board declared a cash dividend of 3% on the Series C Preferred Stock, aggregating approximately $1,275,000 or $31.86 per share. Accordingly, the liquidation value of the Series C Preferred Stock remained at $1,062 per share on December 31, 2023. The dividend was paid on January 17, 2024 to the holders of record of the Company’s Series C Preferred Stock as of January 10, 2024.

Since November 1, 2022, the Company is able to redeem the Series C Preferred Stock at any time, in whole or in part, for an amount based on the liquidation preference per share as in effect at such relieftime. Holders of Series C Preferred Stock have the right to demand that the Company redeem their shares in the event that the Company undergoes a change of control as defined in the Certificate of Designation of the Series C Preferred Stock.

(13)Series C Preferred Stock

In October 2020, the Company issued 40,000 shares of Series C Preferred Stock for an aggregate purchase price of $40.0 million.

As of December 31, 2021, the Board had not declared a cash dividend on the Series C Preferred Stock. Accordingly, during the year ended December 31, 2021, the Company recorded a 5% increase to the liquidation preference of approximately $50 per share of Series C Preferred Stock, aggregating approximately $2,023,000, for a cumulative liquidation value of approximately $42,483,000 ($1,062 per share) as of December 31, 2021. Because a cash dividend of 3% was declared for each of 2023 and 2022, at December 31, 2023 and 2022 there was no change to the liquidation value that was recorded as of December 31, 2021.

As of March 31, 2024, the Board had not yet determined whether to declare a cash dividend at the end of 2024. Accordingly, the Company accrued an accretion at 5% for the quarter on a pro rata basis (approximately $531,000 or $13 per share) and, as a result, the liquidation value of the Series C Preferred Stock was approximately $43,014,000 ($1,075 per share) at March 31, 2024.

There is grantedno prohibition on the repurchase or redemption of Series C Preferred Shares while there is any arrearage in the payment of dividends.

Since the redemption of the Series C Preferred Stock is contingently or optionally redeemable, unless and until we undertake a change of control the Series C Preferred Stock has been classified in mezzanine equity on the Consolidated Balance Sheets.

(14) Cash and Cash Equivalents

The Company defines cash equivalents as highly liquid, short-term investments with original maturities of three months or less. These financial instruments potentially subject the Company to concentrations of credit risk. The Company maintains deposit accounts with several financial institutions. These balances are partially insured by the SEC. Upon further review,Federal Deposit Insurance Corporation (“FDIC”) up to $250,000 per depositor, per FDIC-insured bank, per ownership category. Such deposits may exceed FDIC insurance limits. Although the Company concludedcurrently believes that the SEC was unlikelyfinancial institutions with whom it does business will be able to grant such relieffulfill their commitments to the Company, in 2016. Accordingly, after further consideration, the Company’s Board determined that it would be fair, advisable and in the best interests of the Company and its stockholders to postpone seeking stockholder approval of the Plan of Liquidation and Dissolution until a later time to be determined by the Company’s Board.

If dissolution and liquidation of the Company pursuant to the Plan of Liquidation and Dissolution are approved by the Company’s stockholders and implemented by management, itthere is expected that the Company’s corporate existence will continue for the purpose of winding up its business and affairs through the year 2021, consistent with the expiration of the Company’s existing license arrangements that generate its royalty revenues, unless extended by certain license events occurring. The Company’s future royalty revenues are forecasted to aggregate approximately $11 million from the beginning of 2017 through the end of 2021. This forecast is based upon a variety of estimates and numerous assumptions made by the Company’s management with respect to, among other matters, forecasted sales of the drug products for which the Company has the right to receive royalties and other matters, many of which are difficult to predict, are subject to significant uncertainties, and are beyond the Company’s control. As a result, there can be no assurance that the estimates and assumptions upon which this forecast is based will prove accurate, that the projected resultsthose institutions will be realized or that actual results willable to continue to do so. The Company has not be substantially higher or lower than forecasted.

 9

(11)    Royalty Revenuesexperienced any credit losses associated with its balances in such accounts for the three-month periods ended March 31, 2024 and Accounts Payable

In March 2017, Merck notified2023 and the Company that, during the second and third quarters of 2016, it had made an overpayment to Enzon of approximately $770,000 in royalties (net of a 25% royalty interest that the Company had previously sold). This was due to a previous misunderstanding regarding the date on which the Company’s right to receive royalties from U. S. sales of PegIntron expired, which Merck then advised had occurred in February 2016. Merck notified the Company that it intended to recover such overpayment from the Company by reducing future royalties to which the Company would otherwise be entitled from Merck until the full amount of the overpayment had been recouped. Accordingly, in theyear ended December 31, 2016 financial statements, the Company reduced its previously recorded revenues by the net $770,000 overpayment and recorded a corresponding liability to Merck in accounts payable.2023.

During the three-month period ending March 31, 2017, Merck reported net royalties earned by the Company aggregated approximately $636,000 and withheld that amount as a partial recoupment of its overpayment. That left a balance due to Merck of approximately $134,000 at March 31, 2017.

During the second quarter of 2017, Merck reported net royalties earned by the Company of approximately $335,000. From this amount, Merck would have withheld approximately $134,000, as the balance of the recoupment of the previously reported overpayment. This would have left approximately $201,000 as due to the Company.

However, in the second quarter of 2017, Merck notified the Company that they discovered additional overpayments to the Company resulting from the inaccuracy as to the date on which the Company’s right to receive royalties from various countries’ sales of PegIntron expired. Such net overpayment to Enzon aggregated approximately $563,000 in royalties during 2015 and 2016. Merck notified the Company that it intended to recover such overpayment from the Company by reducing future royalties to which the Company would otherwise be entitled from Merck until the full amount of the overpayment had been recouped. Accordingly, in the June 30, 2017 financial statements, the Company reduced its previously recorded revenues by the net $563,000 overpayment. Merck withheld the $201,000 of the royalties otherwise due for the second quarter of 2017 as a partial recoupment. As a result, the Company recorded the $363,000 remaining to be recouped by Merck as a liability to Merck in accounts payable at June 30, 2017.

In the third quarter of 2017, Merck again notified the Company that, based on rebates and returns of PegIntron products, they had deducted approximately $150,000 from aggregate royalties that were otherwise due to Enzon. This resulted in a net amount due to Enzon of $150,000, which was applied by Merck to the $363,000 liability to Merck. As a result, the Company recorded the $213,000 remaining to be recouped by Merck as a liability to Merck in accounts payable at September 30, 2017.

 10

13

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

Unless the context requires otherwise, references in this Quarterly Report on Form 10-Q to “Enzon,” the “Company,” “we,” “us,” or “our” and similar terms mean Enzon Pharmaceuticals, Inc. and its subsidiaries. The following discussion of our financial condition and results of operations should be read together with our consolidated financial statements and notes to those statements included elsewhere in this Quarterly Report on Form 10-Q and our 2023 Annual Report on Form 10-K.

Forward-Looking Information and Factors That May Affect Future Results

The following discussion contains forward-looking statements within the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. All statements contained in the following discussion, other than statements that are purely historical, are forward-looking statements. Forward-looking statements can be identified by the use of forward-looking terminology such as “believes,” “expects,” “may,” “will,” “should,” “potential,” “anticipates,” “plans,” or “intends” or the negative thereof, or other variations thereof, or comparable terminology, or by discussions of strategy. Forward-looking statements are based upon management’s present expectations, objectives, anticipations, plans, hopes, beliefs, intentions or strategies regarding the future and are subject to known and unknown risks and uncertainties that could cause actual results, events or developments to be materially different from those indicated in such forward-looking statements, including the risks and uncertainties set forth in Item 1A. Risk Factors in our 2023 Annual Report on Form 10-K. These risks and uncertainties should be considered carefully and readers are cautioned not to place undue reliance on such forward-looking statements. As such, no assurance can be given that the future results covered by the forward-looking statements will be achieved.

The percentage changes throughout the following discussion are based on amounts stated in thousands of dollars and not the rounded millions of dollars reflected in this section.

Overview

During 2020, the Company adopted a Section 382 rights plan and completed a Rights Offering, each as further described below. As a result of the successful completion of the Rights Offering, we are positioned as a public company acquisition vehicle, where we can become an acquisition platform and potentially utilize our NOLs and enhance stockholder value. We receive royalty revenues from existing licensing arrangements with other companies primarily related to salesmay acquire businesses, entities or revenue streams that could generate sufficient income so that we can utilize our approximately $102.2 million of four marketed drug products, namely, PegIntron®, Sylatron®, Macugen®federal NOLs. To date, no acquisition candidates have been identified that are in an actionable state and, CIMZIA®. The primary sourcewhile we may be successful in realizing the value of our royalty revenues inNOLs, we cannot assure you that we will be able to do so.

Prior to 2017, is the non-recurring $7.0 million of royalties resulting from our entrance into a Second Amendment (the “Nektar Second Amendment”) to the Company’s Cross-License and Option Agreement (the “Nektar License Agreement”) withNektar Therapeutics, Inc. (“Nektar”). (See below.) Previously, the primary source of our royalty revenues was derived from sales of PegIntron, which is marketed by Merck & Co., Inc. (“Merck”).Merck. We currently have no clinical operations and limited corporate operations.We have no intention of resuming any clinical development activities or acquiring new sources of royalty revenues. Royaltyactivities. We had no revenues from sales of PegIntron accounted for approximately 100% and 61% of our total royalty revenues for the three monthsyear ended September 30, 2017December 31, 2023 and 2016, respectively,the quarters ended March 31, 2024 and approximately 13% and 70% of our total royalty revenue in the nine-month periods ended September 30, 2017 and 2016, respectively, before adjustment for Merck’s recoupment of previously overpaid royalties. The effects of such recoupments were recorded as decreases of royalty revenues aggregating $-0- and $564,000 for the three and nine-month periods ending September 30, 2017, respectively, as discussed in Note 11 to the Condensed Consolidated Financial Statements.

2023.

We were previously dedicated to the research and developmenthave a marketing agreement with Micromet AG, now part of innovative therapeutics for patients with high unmet medical needs. In December 2012, we announced that our Board of Directors with outside consultants began a review of the possible sale or disposition of one or more corporate assets or a sale of our company. At that time, we substantially suspended all clinical development activities with a goal of conserving capital and maximizing value returned to our stockholders. In April 2013, we announced that we had concluded a review of the sale or disposition of one or more corporate assets or a sale of our company. The review did not result in a definitive offer to acquire our company or all or substantially all of our assets. In the same announcement, we also announced that our Board of Directors intended to distribute excess cash, expected to arise from ongoing royalty revenues, in the form of periodic dividends to stockholders.

In June 2015, we delivered notice to Nektar asserting a breach of our Cross-License and Option Agreement with Nektar for Nektar’s failure to pay a post-patent expiration immunity fee that we believe became payable under such agreement. Nektar had disputed our claim to an immunity fee. On August 14, 2015, we filed a summons and complaint against Nektar in the Supreme Court of the State of New York for breach of contractAmgen, Inc. (the “Nektar Litigation”“Micromet Agreement”).

On June 26, 2017, we entered into a Second Amendment to the Nektar License Agreement,wherein Nektar agreed to buy-out all remaining payment obligations to us under the Nektar License Agreement, and in connection therewith, Nektar and we also agreed to settle the Nektar Litigation. In consideration for fully paid-up licenses under the Nektar License Agreement and for the dismissal with prejudice of all claims and counterclaims asserted in the Nektar Litigation, Nektar agreed to pay us the sum of $7.0 million, which satisfies all future obligations of royalty payments, pursuant to the Agreement, the first $3.5 million of which was paid within one business day of the effective date of Nektar Second Amendment and the remaining $3.5 million of which will be paid within one business day of January 5, 2018.

Under our existing agreements with certain third party licensees, we may be entitled to (i) potential futurecertain milestone payments contingent upon the achievement of certain milestones with respect to several drug products in various stages of clinical and preclinical development and (ii) potential future royalty payments relatedif Vicineum, a drug that was being developed by Sesen, Inc., (Sesen”) is approved for the treatment of non-muscle invasive bladder cancer. Sesen announced that it had completed a merger with Carisma Therapeutics Inc. (“Carisma”) and that the combined company will focus on the advancement of Carisma’s proprietary cell therapy for the treatment of cancer and other disorders and that it intends to any future salesseek a partner for the further development of these drug products.  Vicineum.

Due to the challenges associated with developing and obtaining approval for drug products, and the lack of our involvement in the development and approval process, there is substantial uncertainty as to whether any of these milestones will be achieved.  We also have no control over the time, resources and effort that these third party licensees may devote to their programs and limited access to information regarding or resulting from such programs.   Accordingly, there can be no assurance that the Companywe will receive any of the milestone or royalty payments under these agreements. the Micromet Agreement. We will not recognize revenue until all revenue recognition requirements are met.

As part Enzon’s sale of its former specialty pharmaceutical business that was completed in January 2010, weWe may be entitled to certain potential future milestone payments contingent upon the achievement of certain regulatory approval-related milestones with respect to Oncaspar from Shire plc (“Shire”), which assumed the milestone payment obligations when it acquired the Oncaspar product portfolio from Sigma-Tau Finanziaria S.p.A. in July 2015. Based on Shire’s May 2, 2017 investor presentation, we believed that Shire anticipated filing a Biologics License Application (“BLA”) for SC Oncaspar with the FDA in the third quarter of 2017.  As of September 30, 2017, there has been no public announcement by Shire of any such filing. If such filing is made and FDA approval is obtained for SC Oncaspar, under our agreement, we would be entitled to a milestone payment of $7.0 million. There can be no assurance that Shire will file a BLA for SC Oncaspar with the FDA or that the FDA will approve the BLA, if filed.  Accordingly, there can be no assurancethird-party licensees. We cannot assure you that we will receive any of the milestone payments related to SC Oncaspar or any other such milestone payments resulting from our agreements with any of Enzon’s other third party licensees.our third-party licensees or that any sales of related products will be made. We will not recognize revenue until notification from Shire orany of our other third partythird-party licensees that the conditions necessitating payment of the milestone were satisfied and collection of the milestone payment is reasonably assured. until all revenue recognition requirements are met.

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14

Acquisition Activities

Commencing on March 1, 2016, we changed the location of our principal executive offices to 20 Commerce Drive, Suite 135, Cranford, New Jersey, 07016. We entered into an office service agreement with Regus Management Group, LLC (“Regus”) for use of office space at this location effective March 1, 2016. Under the agreement, in exchange for our right to use the office space at this location, the Company was required to pay Regus an initial service retainer of $2,418 and thereafter pay Regus a monthly fee of $1,209 until February 28, 2017. This agreement was renewed for another year, until February 28, 2018, for a monthly fee of $1,229.

We wound down our remaining research and development activities during 2013. We have no intention of resuming any clinical development activities or acquiring new sources of royalty revenues.

Plan of Dissolution

On February 4, 2016, ourOur Board of Directors adopted a Plan of Liquidation and Dissolution (the “Plan of Liquidationour management are actively involved in pursuing, sourcing, reviewing and Dissolution”), pursuant to which the Company would, subject to obtaining requisite stockholder approval, be liquidatedevaluating various potential acquisition transactions consistent with our long-term strategy. Our management and dissolved in accordance with Sections 280 and 281(a) of the General Corporation Law of the State of Delaware. In approving the Plan of Liquidation and Dissolution, our Board of Directors had considered, among other factors, the abilityhave made a number of the Companycontacts and engaged in discussions with principals of individual companies and financial advisors on behalf of various individual companies, while continuing to obtain no-action relief from the Securities and Exchange Commission (the “SEC”)evaluate potential transactions. To date, we have not developed any actionable transactions. We will continue to suspend certain of the Company’s reporting obligations under the Securities Exchange Act of 1934, as amended, and the anticipated cost savings if such relief is granted by the SEC. Upon further review, we concluded that the SEC was unlikely to grant such relief to the Company in 2016. Accordingly, after further consideration, our Board of Directors determined that it would be fair, advisable and in the best interests of the Company and its stockholders to postpone seeking stockholder approval of the Plan of Liquidation and Dissolution until a later time to be determined by our Board of Directors.

If dissolution and liquidation of the Company pursuant to the Plan of Liquidation and Dissolution are approved byupdate our stockholders and implemented by us, we expect the Company’s corporate existence to continue for the purpose of winding up its business and affairs through the year 2021, consistent with the expiration of our existing license arrangements that generate our royalty revenues. Our future royalty revenues are forecasted to aggregate approximately $11 million from the beginning of 2017 through the end of 2021. This forecast is based upon a variety of estimates and numerous assumptions made by our management with respect to, among other matters, forecasted sales of the drug products for which we have the right to receive royalties and other matters, many of which are difficult to predict, are subject to significant uncertainties, and are beyond our control. As a result, there can be no assurance that the estimates and assumptions upon which this forecast is based will prove accurate, that the projected results will be realized or that actual results will not be substantially higher or lower than forecasted.

 12

as material developments arise.

Throughout this Management’s Discussion and Analysis, the primary focus is on our results of operations, cash flows and financial condition. The percentage changes throughout the following discussion are based on amounts stated in thousands of dollars and not the rounded millions of dollars reflected in this section.

dollars.

Results of Operations

Revenues:

Royalties  (in millions of dollars):

  Three Months Ended
September 30,
  Nine Months Ended
September 30,
 
  2017  %
Change
  2016  2017  %
Change
  2016 
Royalty revenue $.15   93% $2.0  $8.9   19% $7.5 
Less: Recoupment by Merck  -   N/A   -   (0.6)  N/A   - 
  $.15   93% $2.0  $8.3   11% $7.5 

Royalty revenues related to the Nektar Second Amendment aggregated $7.0 million in the second quarter of 2017. Royalty revenues from sales of PegIntron were negative in the second quarter of 2017 due to the recoupment by Merck of previously overpaid royalties and accounted for approximately 100% and 61% of our total royalty revenues forIn the three months ended September 30, 2017March 31, 2024 and 2016, respectively,2023, we earned no milestone or royalty revenues.

Interest and 13% and 70% (before recoupment) of our total royalty revenues for the nine-month periods ended September 30, 2017 and 2016, respectively. Aside from the negative effects of the recoupments and substantial product returns and rebates Dividend Income (in the third quarter of 2017, royalty revenues from Merck have been declining sharply. There are multiple oral drug therapies, both available and in development, that have been effective for treatment of hepatitis C that do not require interferon. As a result, it is likely that sales of PegIntron-related products will continue their declining trend.  

The following table summarizes our PegIntron royalties earned (in millionsthousands of dollars):

Three Months Ended March 31,

%  

    

2024

    

Change

    

2023

Interest and dividend income

$

647

45

$

447

  Three Months Ended        Nine Months Ended       
  September 30,  Dollar  Percent  September 30,  Dollar  Percent 
PegIntron royalties
from:
 2017  2016  Change  Change  2017  2016  Change  Change 
US sales $(0.09) $0.30  $(0.39)  (128)% $(0.12) $0.88  $(1.00)  (114)%
Foreign sales - Europe  0.17   0.12   0.05   40%  0.59   1.03   (0.44)  43%
Foreign sales - Japan  0.00   0.01   (0.01)  (79)%  (0.05)  0.04   (0.09)  (225)%
Foreign sales - Other  0.07   0.78   (0.71)  (92)%  0.70   3.25   (2.55)  (78)%
Total $0.15  $1.21  $(1.06)  (88)% $1.12  $5.20  $(4.08)  (78)%
Less: Recoupment by Merck  -   -           (0.56)  -  $(0.56)    
  $0.15  $1.21  $(1.06)     $0.56  $5.20  $(4.71)    

Our future revenues are heavily weighted towards royaltiesInterest and revenuesdividend income is attributable to bethe interest and dividends received on the invested cash and cash equivalents we received from the use$43.6 million of proceeds from our technologyrights offering (see Note 12 to our Consolidated Financial Statements). Interest and are dependent upon numerous factors outsidedividend income increased by approximately $200,000, or 45%, to $647,000 for the first quarter of our control. Other than2024 from $447,000 for the non-recurring royalties resulting fromcomparable period in 2023. The increase in other income is attributable to the Nektar Second Amendment and potential future milestone payments with others, a significant portionhigher rates of our royalty revenues is dependent upon sales of PegIntron, which have been in decline since 2008 and which recently suffered from returns and rebates. Merck’s obligation to pay us royalties on sales of PegIntron terminates, on a country-by-country basis, upon the later of the date on which the last patent to contain a claim covering PegIntron expiresinterest in the country or 15 years after the date on which PegIntron was first approved for commercial marketing in such country. Our rights to receive royalties from sales of PegIntron expired in the U.S. in 2016 and are expected to expire in Europe in 2018 and in Japan in 2021.

Other factors potentially affecting our royalty revenues include new or increased competition from products that may compete with the products for which we receive royalties and the effectiveness of marketing by our licensees.

On June 26, 2017, we entered into a Second Amendment to our Cross-License and Option Agreement with Nektar wherein Nektar agreed to buy-out all remaining payment obligations to us under the Cross-License and Option Agreement, and in connection therewith, Nektar and we also agreed to settle prior litigation in which we had alleged a breach of contract for Nektar’s failure to pay a post-patent expiration immunity fee that we believe became payable under the Cross-License and Option Agreement. In consideration for fully paid-up licenses under the Cross-License and Option Agreement and for the dismissal with prejudice of all claims and counterclaims asserted in the litigation, Nektar agreed to pay us the sum of $7.0 million, which satisfies all future obligations of royalty payments pursuant to the Cross-License and Option Agreement, the first $3.5 million of which was paid within one business day of the effective date of the Second Amendment and the remaining $3.5 million of which will be paid within one business day of January 5, 2018. Accordingly, the Company recorded revenue of $7.0 million and an account receivable of $3.5 million in the second quarter of 2017. 

 13

Miscellaneous Income

There was no miscellaneous income for the three-month and nine-month periods ended September 30, 2017.

Miscellaneous income was approximately $63,000 and $21,000 for the nine months and three months ended September 30, 2016, respectively, and related, primarily,2024 compared to sublease income.

2023.

Operating Expenses:

General and Administrative (in millionsthousands of dollars):

    

Three Months Ended March 31,

    

    

Percent

    

2024

Change

2023

General and administrative

$

326

14

%

$

285

  Three Months Ended September 30,  Nine months Ended September 30, 
  2017  %
Change
  2016  2017  %
Change
  2016 
General and administrative $0.34   (11) $0.38  $1.02   (34) $1.55 

General and administrative expenses in the three months ended September 30, 2017 declinedincreased by approximately $41,000, or 11%14%, to $335,000 from $376,000approximately $326,000 for the thirdfirst quarter of 2016.2024 from approximately $285,000 for the first quarter of 2023. The decreaseincrease in general and administrative expense is substantially attributable to the approximate $50,000 decrease in corporate filings in 2017, as compared with 2016, as partially offset by a net increase in office expenseprofessional fees.

Tax Expense:

Assuming no acquisition is completed or material changes in results through March 2025, the Company has partially reversed the valuation allowances as of March 31, 2024. Deferred tax benefits of $1,000 and contracted services.

General$36,000, respectively were recorded during the quarters ended March 31, 2024 and administrative expenses in the nine months ended September 30, 2017 decreased by approximately $532,000, or 34%, to $1.02 million from $1.55 million for the first nine months of 2017. The decrease in expense is substantially attributable2023. (See Note 8 to the decrease in rent expense, utility costs and general insurance expense in connection with our lease termination as well as a decrease in professional fees, primarily legal and accounting fees, incurred in 2016 in connection with the Plan of Liquidation and Dissolution that was adopted in February 2016.

Tax Expense:

We incurred a tax expense of approximately $2.4 million in the first nine months of 2017, of which approximately $0.3 million in income tax benefit was incurred during the third quarter of 2017. The effective tax rate for the nine months ended September 30, 2017 was 32.2%, compared with 41.7% for the corresponding period in the prior year. The reduction in the effective tax rate is attributable to the increase in projected income for the current year, of $3.9 million, which included the effect of the $7 million in revenues related to the Second Amendment with Nektar. In addition, we recorded tax expense of $1.4 million as a discrete item in the second quarter of 2017 for the tax effect of a decrease in the beginning of the year projection of income to be available in future years.

Condensed Consolidated Financial Statements.)

Liquidity and Capital Resources

Our current sourcessource of liquidity areis our (i)existing cash on hand, which includes the approximately $43.6 million of gross proceeds from our Rights Offering and (ii) anticipated royalty revenues from third-party sales of marketed drug productsthe interest earned on that utilize our proprietary technology, includingamount. (See Note 12 to the remaining $3.5 million due from Nektar in January 2018.Condensed Consolidated Financial Statements.) While we no longer have any research and development activities, we continue to retain rights to receive royalties and milestone payments from existing licensing arrangements with other companies.companies and, accordingly, we may be entitled to a share of milestone and royalty payments from the approval and sale of Vicineum, We believe that our existing cash on hand collection of the $3.5 million receivable from Nektar and anticipated royalty revenues, will be sufficient to fund our operations, at least, through November 15, 2018. However, ourApril 2025. Our future royalty revenues are expected to decrease sharplybe de minimis over the next several years and there can be no assurancewe cannot assure you that we will receive amounts ofany royalty, revenues as anticipated.

Under our existing agreements with certain third party licensees, we may be entitled to (i) potential future milestone payments contingent upon the achievement of certain milestones with respect to several drug products in various stages of clinical and preclinical development and (ii) potential future royalty payments related to any future sales of these drug products.  Due to the challenges associated with developing and obtaining approval for drug products, there is substantial uncertainty whether any of these milestones will be achieved.  We also have no control over the time, resources and effort that these third party licensees may devote to their programs and limited access to information regarding or resulting from such programs.   Accordingly, there can be no assurance that the Company will receive any of the milestone or royalty payments under these agreements. other revenues.

15

While we are positioned as a public company acquisition vehicle, where we can become an acquisition platform and more fully utilize our NOLs and enhance stockholder value, we cannot assure you that we will succeed in making acquisitions that are profitable and that will enable us to utilize our NOLs.

Cash provided by operating activities represents a net income, as adjusted for certain non-cash items including the effect of changes in operating assets and liabilities. Cash provided by operating activities during the three months ended March 31, 2024 was $4.3 million as of September 30, 2017,approximately $251,000, as compared to $7.6 million as of December 31, 2016. The decrease of approximately $3.3 million was primarily attributable to the net cash provided by operating activities of approximately $3.3 million, as partially offset by cash$170,000 during the comparable period in 2023. The increase of approximately $81,000 was primarily attributable to interest income of approximately $647,000 in the first quarter of 2024, resulting in net income of approximately $320,000 during that quarter compared to net income of approximately $197,000 during the first quarter of 2023.

Cash used in financing activities represents cash dividends of $6.6 million in connection with the special cash dividend that wasapproximately $1,275,000 paid to shareholders in September 2017.holders of the Company’s Series C Preferred Stock.

The net effect of the foregoing was a decrease of cash and cash equivalents of approximately $1.0 million, from $47.0 million at December 31, 2023 to $46.0 million at March 31, 2024.

Off-Balance Sheet Arrangements

As part of our ongoing business, we do not participate in transactions that generate relationships with unconsolidated entities or financial partnerships, such as entities often referred to as structured finance or special purpose entities (SPEs), which would have been established for the purpose of facilitating off-balance sheet arrangements or other contractually limited purposes. As of September 30, 2017,March 31, 2024, we were not involved in any SPE transactions.

 14

Critical Accounting Policies and Estimates

A critical accounting policy is one that is both important to the portrayal of a company’s financial condition and results of operations and requires management’s most difficult, subjective or complex judgments, often as a result of the need to make estimates about the effect of matters that are inherently uncertain.

Our consolidated financial statements are presented in accordance with accounting principles that are generally accepted in the United StatesU.S.  (“U.S. GAAP”). All applicable U.S. GAAP accounting standards effective as of September 30, 2017March 31, 2023 have been taken into consideration in preparing the consolidated financial statements. The preparation of the consolidated financial statements requires estimates and assumptions that affect the reported amounts of assets, liabilities, revenues, expenses and related disclosures. Some of those estimates are subjective and complex, and, consequently, actual results could differ from those estimates. The following accounting policies and estimates have been highlighted as significant because changes to certain judgments and assumptions inherent in these policies could affect our consolidated financial statements.

We base our estimates, to the extent possible, on historical experience. Historical information is modified as appropriate based on current business factors and various assumptions that we believe are necessary to form a basis for making judgments about the carrying value of assets and liabilities. We evaluate our estimates on an ongoing basis and make changes when necessary. Actual results could differ from our estimates.

Revenues

Royalties under our license agreements with third-parties and pursuant to the sale of our former specialty pharmaceutical business are recognized when reasonably determinable and earned through the sale of the product by the third-party and collection is reasonably assured. Notification from the third-party licensee of the royalties earned under the license agreement is the basis for royalty revenue recognition. This information generally is received from the licensees in the quarter subsequent to the period in which the sales occur.

Income Taxes

Under the asset and liability method of accounting for income taxes, deferred tax assets and liabilities are recognized for the estimated future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. A valuation allowance on net deferred tax assets is provided for when it is more likely than not that some portion or all of the deferred tax assets will not be realized. As of September 30, 2017,March 31, 2024, we believe, based on our projections, that ita partial reversal of the valuation allowance is more likely thannecessary. Interest rates may fluctuate throughout 2024 and during the first quarter of 2025, however, they are not expected to return to low rates of the past creating a projected taxable income position. Therefore, the Company will partially reverse the valuation allowances. We are positioned as a public company acquisition vehicle, where we can become an acquisition platform and potentially utilize our NOLs. We may acquire businesses, entities or revenue streams that except for $1.7could generate sufficient income so that we can utilize our approximately $102.2 million of net operating losses,federal NOLs. At this time, however, we cannot assure you that we will be successful in doing so. Accordingly, our deferred tax assets, includingmanagement will continue to assess the remaining net operating losses from operating activitiesneed for this valuation allowance and stock option exercises,will make

16

adjustments when appropriate. Additionally, our management believes that our NOLs will not be realized. limited by any changes in our ownership as a result of the successful completion of the Rights Offering (See Note 12 to the Consolidated Financial Statements).

We recognize the benefit of an uncertain tax position that we have taken or expect to take on the income tax returns we file if it is more likely than not that we will be able to sustain our position.

 15

Forward-Looking Information and Factors That May Affect Future Results

This Quarterly Report on Form 10-Q contains forward-looking statements within the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. All statements contained in the Quarterly Report on Form 10-Q, other than statements that are purely historical, are forward-looking statements. Forward-looking statements can be identified by the use of forward-looking terminology such as the words “believes,” “expects,” “may,” “will,” “should,” “potential,” “anticipates,” “plans” or “intends” or the negative thereof, or other variations thereof, or comparable terminology, or by discussions of strategy. Forward-looking statements are based upon management’s present expectations, objectives, anticipations, plans, hopes, beliefs, intentions or strategies regarding the future and are subject to known and unknown risks and uncertainties that could cause actual results, events or developments to be materially different from those indicated in such forward-looking statements, including, but not limited to, the following risks and uncertainties:

We may be unsuccessful in our strategy to fully utilize our NOLs and other tax assets and enhance stockholder value as a public company acquisition vehicle.

·The proposed dissolutionOur sources of revenue are limited and, liquidationas a result of our cash reserves, we expect only limited revenue and profitability for the Company may not be completed in a timely manner or at all.foreseeable future.

·The amountIn recent years, we distribute to our shareholders as liquidating distributions, if any, pursuant to the Plan of Liquidation and Dissolution may be substantially less than estimated.

·We derive a significant portionderived most of our royalty revenues from continued sales of PegIntron, which have been in decline since 2008, in part, because there are multiple oral drug therapies, both availablesharp decline. In addition, our right to receive royalties on U.S. and in development, that have been effective for treatment of hepatitis C that do not require interferon, and ifEuropean sales of PegIntron continue to decline or sales of other drug products forexpired in 2016 and 2018, respectively, which we receivehas negatively impacted our royalty revenues materially decline, our results of operations and financial position could be materially harmed.revenues.

·We may not be able to sustain profitability and we may incur losses over the next several years.

·Our rights to receive royalties on sales of PegIntron and sales of other drug products have expired in various jurisdictions and, except for Vicineum, will, eventuallyby 2024, expire and weworld-wide. We currently do not intend on acquiringanticipate any significant royalties from other sources, but we may acquire new sources of royalty revenues.

·WeThe unprecedented actions taken globally to control the spread of COVID 19 and its related variants, as well as the uncertainty surrounding the success of global vaccination efforts, may not realizematerially and adversely affect our deferred income tax assets.future right to receive licensing fees, milestone payments and royalties on product candidates that are being developed by third parties.

·We have reallocated all employment responsibilities and outsourced all corporate functions, which makemakes us more dependent on third-partiesthird parties to perform these corporate functions.

·We may be subject to a variety of types of product liability or other claims based on allegations that the use of our product candidates by participants in our previously conducted clinical trials has resulted in adverse effects, and our insurance may not cover all product liability or other claims.

·Our revenues largely depend on patents and proprietary rights, which may offer only limited protection against potential infringement and the development of competing products.

·We are party to license agreements whereby we may receive royalties and or milestone payments from products subject to regulatory approval.

·The price of our common stock has been, and may continue to be, volatile.

·Our common stock is quoted on the OTCQX market of the OTC Markets Group, Inc., which has a very limited trading market and, therefore, market liquidity for our common stock is low and our stockholders’ ability to sell their shares of our common stock may be limited.

17

·The declaration of dividends is within the discretion of our Board of Directors, subject to any applicable limitations under Delaware corporate law, as well as the requirements of the Series C Preferred Stock. Our ability to pay dividends in the future depends on, among other things, our fulfillment of the conditions of the Series C Preferred Stock, fluctuating royalty revenues, our ability to acquire other revenue sources and our ability to manage expenses, including costs relating to our ongoing operations.
We have adopted a Section 382 rights plan, which may discourage a corporate takeover.
Anti-takeover provisions in our charter documents and under Delaware corporate law may make it more difficult to acquire us, even though such acquisitions may be beneficial to our stockholders.
The terms of our outstanding Series C Preferred Stock and the issuance of additional series of preferred stock may adversely affect rights of our common stockholders.
The interests of our significant stockholders may conflict with the interests of other stockholders.
If we experience an "ownership“ownership change," as defined in Section 382 of the Internal Revenue Code of 1986, as amended, our ability to fully utilize our net operating loss carryforwards (“NOLs”)NOLs on an annual basis will be substantially limited, and the timing of the usage of the NOLs could be substantially delayed, which could therefore significantly impair the value of those benefits.

 16If we experience a “Change of Control,” as defined in Certificate of Designation of the Series C Preferred Stock, the holders of the Series C Preferred Stock shall have the right, at such holder’s option, to require the Company to redeem at the Liquidation Preference then in effect all or a portion of such holder’s shares of Series C Preferred Stock, which would negatively impact our available cash.

·The declaration of dividends is within the discretion of our Board of Directors, subject to any applicable limitations under Delaware corporate law. Our ability to pay dividends in the future depends on, among other things, our future royalty revenues, which are expected to decrease sharply over the next several years, as well as our ability to manage expenses, including costs relating to our ongoing operations.

·Anti-takeover provisions in our charter documents and under Delaware corporate law may make it more difficult to acquire us, even though such acquisitions may be beneficial to our stockholders.

·The issuance of preferred stock may adversely affect rights of our common stockholders.

A more detailed discussion of these risks and uncertainties and other factors that could affect results is contained in our filings with the U.S. Securities and Exchange Commission,SEC, including in Item 1A. “Risk Factors” of our Annual Report on Form 10-K for the year ended December 31, 2016, as updated in “Item 1A. Risk Factors” of our subsequent quarterly reports on Form 10-Q.2023. These risks and uncertainties and other factors should be considered carefully and readers are cautioned not to place undue reliance on such forward-looking statements. As such, no assurance can be given that the future results covered by the forward-looking statements will be achieved. All information in this Quarterly Report on Form 10-Q is as of the date of this report, unless otherwise indicated, and we undertake no duty to update this information.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

As a smaller reporting company, we are not required to provide information required by this item.

Item 4. Controls and Procedures.

Evaluation of Disclosure Controls and Procedures

Our management, under the directionconsisting of Richard L. Feinstein who serves as our Chief Executive Officer and Chief Financial Officer, has evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), as of September 30, 2017.March 31, 2024. Disclosure controls and procedures are designed to ensure that information required to be disclosed in reports filed or submitted under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in SEC rules and forms and that such information is accumulated and communicated to management, including the Chief Executive Officer and Chief Financial Officer, to allow timely decisions regarding required disclosures. The Company’sBased on that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that, as of September 30, 2017,March 31, 2024, the Company’s disclosure controls and procedures were effective.

Changes in Internal Control Over Financial Reporting

There were no changes in our internal control over financial reporting as such term is defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act, during the quarter ended September 30, 2017March 31, 2024 that have materially affected, or are reasonably likely to materially affect our internal control over financial reporting.

 17

18

Part II – OTHER INFORMATION

Item 1. Legal Proceedings

We are not currently a party to any lawsuit or proceeding which, in the opinion of management, is likely to have a material adverse effect on us or our business.

Item 1A. Risk Factors.

There are no material changes from the risk factors previously disclosed in our Annual Report on Form 10-K for the fiscal year ended December 31, 20162023 filed with the SEC on March 24, 2017.20, 2024.

Item 2.Unregistered Sales of Equity Securities and Use of Proceeds.

Proceeds

None.

Item 3. Defaults Upon Senior Securities

None.

Item 4. Mine Safety Disclosures

Not applicable.

Item 5. Other Information

None.

Item 6. Exhibits.

Exhibits

(a) Exhibits required by Item 601 of Regulation S-K.

Exhibit
Number
Description
Reference
No.
31.1

Exhibit
Number

Description

Reference
No.

31.1

Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002  

+
31.2Certification ofand Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002  2002*

+

32.1

Certification of Principal Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*  

+
32.2Certification ofand Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*

+

101

101.INS

The following materials from Enzon Pharmaceuticals, Inc.’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2017, formatted

Inline XBRL Instance Document

+

101.SCH

Inline XBRL Taxonomy Extension Schema Document

+

101.CAL

Inline XBRL Taxonomy Extension Calculation Linkbase Document

+

101.DEF

Inline XBRL Taxonomy Extension Definition Linkbase Document

+

101.LAB

Inline XBRL Taxonomy Extension Label Linkbase Document

+

101.PRE

Inline XBRL Taxonomy Extension Presentation Linkbase Document

+

104

Cover Page Interactive Data File (formatted as inline XBRL with applicable taxonomy extension information contained in XBRL (Extensible Business Reporting Language): (i) Condensed Consolidated Balance Sheets, (ii) Condensed Consolidated Statements of Comprehensive Income (Loss), (iii) Condensed Consolidated Statements of Cash Flows, and (iv) Notes to Condensed Consolidated Financial Statements.  Exhibits 101)

+

++Filed herewith.

*These certifications are not deemed filed by the Commission and are not to be incorporated by reference in any filing the Company makes under the Securities Act of 1933 or the Securities Exchange Act of 1934, irrespective of any general incorporation language in any filings.

 18
*This certification is not deemed filed by the Commission and is not to be incorporated by reference in any filing the Company makes under the Securities Act of 1933 or the Securities Exchange Act of 1934, irrespective of any general incorporation language in any filings.

19

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

ENZON PHARMACEUTICALS, INC.

(Registrant)

Dated: November 9, 2017

/s/ Andrew Rackear

Dated:May 10, 2024

Andrew Rackear
Chief Executive Officer and Secretary
(Principal Executive Officer)
Dated: November 9, 2017

/s/ Richard L. Feinstein

Richard L. Feinstein

Vice President-Finance and

Chief Executive Officer, Chief Financial Officer and Secretary

(Principal Financial Officer)

 19

EXHIBIT INDEX

 

Exhibit
Number  
Description  Reference
No.
31.1Certification of

(Principal Executive Officer, pursuant to Section 302 of the Sarbanes-Oxley Act of 2002  

+
31.2Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002  +
32.1Certification ofand Principal Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*  +
32.2Certification of Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*  +
101The following materials from Enzon Pharmaceuticals, Inc.’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2017, formatted in XBRL (Extensible Business Reporting Language): (i) Condensed Consolidated Balance Sheets, (ii) Condensed Consolidated Statements of Comprehensive Income (Loss), (iii) Condensed Consolidated Statements of Cash Flows, and (iv) Notes to Condensed Consolidated Financial Statements.  +Accounting Officer)

+Filed herewith.

*These certifications are not deemed filed by the Commission and are not to be incorporated by reference in any filing the Company makes under the Securities Act of 1933 or the Securities Exchange Act of 1934, irrespective of any general incorporation language in any filings.

 20

20